Bristol Myers Squibb Manager Clinical Research Csc-Med Writ in SHINJUKU, Japan
-A senior level scientific writer/manager (i.e., player/coach model) who creates clinical/regulatory documents, ensuring the coordination and integration of the scientific, medical, and regulatory input from development team members.
-Participate in relevant filing subteam(s) and take a proactive strategic role in positioning content in submission-level documents for assigned projects.
-Drive continuous process improvements by identifying and simplifying processes. Leads implementation of business process improvements based on information from collected metrics.
-Supervise other scientific writers and improves their capabilities in creation of clinical/regulatory documents for Japan.
-Provide additional value by creating better collaborative work environment internally and externally to ensure that Japan team has a good communication with HQ counterparts as well as key stakeholders, such as clinical research and regulatory.-Comply with internal and external processes and guidelines while managing the review process and, on an ongoing basis, resolve issues, errors, or inconsistencies with pertinent team members to ensure timely completion and high quality of assigned documents.
We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.
Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.